54704-34-6

Basic information

• Product Name: 2-AMINO-3-CYCLOHEXYLPROPANE
• Synonyms: 2-AMINO-3-CYCLOHEXYLPROPANE;1-cyclohexylpropan-2-amine;L-1-methyl-2-cyclohexylethylamine
• CAS NO: 54704-34-6
• Molecular Formula: C₉H₁₉N
• Molecular Weight: 141.25
• Mol File: 54704-34-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 181.5°C at 760 mmHg
• Flash Point: 58.3°C
• Appearance: /
• Density: 0.858g/cm³
• Vapor Pressure: 0.848mmHg at 25°C
• Refractive Index: 1.46
• CAS DataBase Reference: 2-AMINO-3-CYCLOHEXYLPROPANE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-3-CYCLOHEXYLPROPANE(54704-34-6)
• EPA Substance Registry System: 2-AMINO-3-CYCLOHEXYLPROPANE(54704-34-6)

Safety Data

• Hazardous Substances Data: 54704-34-6(Hazardous Substances Data)

Usage

General Description

2-AMINO-3-CYCLOHEXYLPROPANE is a chemical compound with the molecular formula C9H19N. It is a cyclic amine that consists of a cyclohexane ring attached to a three-carbon chain with an amino group. 2-AMINO-3-CYCLOHEXYLPROPANE is used in organic synthesis and pharmaceutical research as a building block in the production of various organic compounds. It also has potential applications in the field of medicinal chemistry, as it can be used in the development of new drugs and pharmaceutical products. Additionally, 2-AMINO-3-CYCLOHEXYLPROPANE may have industrial uses in the production of specialty chemicals and as a reagent in chemical processes.

InChI:InChI=1/C9H19N/c1-8(10)7-9-5-3-2-4-6-9/h8-9H,2-7,10H2,1H3

Upstream product

• 2043-61-0 cyclohexanecarbaldehyde 
• 26226-49-3 1-methyl-2-cyclohexyl nitroethylene 
• 17019-26-0 (E)-2-(hydroxyimino)-1-phenylpropan-1-one 
• 103-78-6 4-cyclohexyl-butan-2-one 
• 17322-34-8 (2-nitropropyl)benzene 
• 60-15-1 2-amino-1-phenylpropane 
• 768-50-3 1-cyclohexenylacetone 

Downstream Products

• 1351781-84-4 C₁₂H₂₃NO₂ 
• 5913-12-2 (S)-(+)-1-cyclohexyl-2-propanamine 
• 52617-05-7 (R)-(-)-1-cyclohexyl-2-propanamine 

Relevant articles and documents

Enzymatic enantiomeric resolution of phenylethylamines structurally related to amphetamine

Both enantiomers of several phenylethylamines, structurally related to amphetamine, have been prepared in good yields and excellent enantiomeric purity by enzymatic kinetic resolution using CAL-B and ethyl methoxyacetate as the acyl donor. In the case of the 4-hydroxyderivative of amphetamine (compound 4i), the S enantiomer racemized possibly in a dynamic kinetic resolution (DKR) under the enzymatic conditions used. The Royal Society of Chemistry 2011.

Preparation of esters of phosphorus acids

Esters of phosphorus acids are prepared by an improved process whereby aromatic alcohols and phosphorus halides are reacted at specified temperatures in the presence of amine catalysts thereby providing high yields of substantially pure esters and allowing preparation of selected halogen-containing mono- and di-esters of phosphorus acids wherein halogen is directly bonded to phosphorus having substantially no side reactant contamination. The phosphorus esters are useful as intermediates in the preparation of plasticizers, oil additives and functional fluids.